ZMP
si:dkey-102c8.6
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC556445 [Source:RefSeq peptide;Acc:NP_001077294]
Human Orthologue:
GLS2
Human Description:
glutaminase 2 (liver, mitochondrial) [Source:HGNC Symbol;Acc:29570]
Mouse Orthologue:
Gls2
Mouse Description:
glutaminase 2 (liver, mitochondrial) Gene [Source:MGI Symbol;Acc:MGI:2143539]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa32379 | Nonsense | Available for shipment | Available now |
| sa39358 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa29725 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa30726 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32379
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000031005 | Nonsense | 113 | 542 | 4 | 18 |
| ENSDART00000147580 | Nonsense | 197 | 627 | 4 | 18 |
Genomic Location (Zv9):
Chromosome 22 (position 10217271)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 10077439 |
| GRCz11 | 22 | 10107121 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCATTTGTGGACATCATCAATCACATTTATTACACATCAAAACTGCAA[C/T]AAGATGGACAGGTAAGATGTGTATTTTATTACCTCACTTTATGTACTTAA
Long Flanking Sequence:
CTTTAAAAAGAACATTCTGTGAGCTATAAACTGTTACGTTATTGTTATAGCTGTGGTGTGGATTCTGCAATTTGTCTAAATGTATTAAAACCTTTATTATTATTGGTATAGTTATCATGAATGTGAACAATGAAGAGAAAGAACAGTATTTTCTGTATCTTACAGGCTTTGAAAAGCACCGGATTGCTGACTTCTGATCCAAGATTACGAGACTGTATGGAAAAAATTCGCAGAGCTGTCCGAGATTCGACTGGTGAGGTCATGATGGACCGCGAGCTATTCAAAAAGCGAGTATATTGTGTTTTAAAACAAAACAAATTTCCTACAAAAATAAGTGTATTTATATAGTGACTAAGTTGCAAAAGTTTCCGACGTTATACAGATGTGCAAGTGGCAACATTGTTCTCCTGAGTCTCGCTTTCAGACGAAAGTTCATCATTCCTGAATTTGAGGCATTTGTGGACATCATCAATCACATTTATTACACATCAAAACTGCAA[C/T]AAGATGGACAGGTAAGATGTGTATTTTATTACCTCACTTTATGTACTTAATTGAATAGTACTCATTTAGTTTTTTTTTAGGTTGCGAAATACATTCCCCATCTAACCAAGTTCAGTCCTGATCTTTGGGGCGTCTCATTGTGCACAGTGGATGGACAAAGGTAAATTTATAAAACGAAACACGGCCTCCAGACATTTGCGAATATTCTGAATAGGGCTGTACAATATATTGTTTTAGCATCGATTTCACAACGTGATCATTTACAATACGCAATACGTATACGCTATGTTAAGTCTAAATTTTATAGTTGATCATTTTACAAGTGTTTTTGAGGCCTGTGACTGTGTGAGGGTTTTAAAAGCATTCAGGCCTAAGAGTTTTGGCATTTGTAACTTTGACAAATTAATAACAATTTAATTGTTTATAAAACAAAAGATGATGCAGTATTATTTTACATTTTATTATTTGATTATTCAACAATCAAACACTTTTTATTTAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39358
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000031005 | Essential Splice Site | 247 | 542 | 9 | 18 |
| ENSDART00000147580 | Essential Splice Site | 332 | 627 | 9 | 18 |
Genomic Location (Zv9):
Chromosome 22 (position 10214785)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 10074953 |
| GRCz11 | 22 | 10104635 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTGTTAAGAAGATGACAGGCAGTGAGTACGTGGGCTTCAGCAACGCAAC[G/A]TATGTCTTATTAGTTTGATATTCTAAGCTTGTTTCCACCTGTTGACTCAC
Long Flanking Sequence:
ATTCCAGCCTGCCTTTATTACATTTATAACTTATATGTGTTCTTTATTGGACCAAAAATTATACTTAATTGGAACAAGGCCTATTCATCTGTACAGCCAAAAAAGTAGTGCACACCACCTTTTTGCTATATCATAAAGTCAATGTTATTTACCTTTTTTAAAAATTATCTGTTTATTTGGGACACTTTAATTCCATAATAAAAGATTCTTTGTCTTGAAAATATTTGCTTTAGATTGTGAAATTGTTCTTCATACCGCTAAAACATTGTTGAGGGAATCAATTGTTATTCATTTACATCATAATTTATAAAAACCCATTTACGATTCTTCGCAGTACTTTAAATTTTAATAGTGTATGTGTCTGTGAACTTTTTCATTCAATAGACCAGATGCTATTTCAAATTTGGTAGTTGCACTGATTTTGTTGGGTCTCAATTTTAGGTAATGGACTTTGTTAAGAAGATGACAGGCAGTGAGTACGTGGGCTTCAGCAACGCAAC[G/A]TATGTCTTATTAGTTTGATATTCTAAGCTTGTTTCCACCTGTTGACTCACTATTGACTCATCTGATTTTGTTTGAACAGGTTCCAGTCAGAAAAGGAGACAGGAGACAGAAACTATGCAATAGGATACTACCTAAAAGAGAAAAAGGTTACTTAAAGAAACAATAGCTATGTTTCCATCCAAAGATGCTAATTAAAATTATGTGCAAAACTGGAATATCACATAAAACATTTGCAAAAAAACATTGTTTCCATCCAGTGAGTCAAAATGTTCACTTCCTGATAAACTGAAGCCAAATTTCAAAAAGAGAAATTAATTTACTGTGCTAGAGGAAACCACTGGGGGCCTTCTTTCTTACACAATAAATTACTAGTAAAGAGATTATTATGGGAGCATAGATACTCAAGTCAGTTCTGAGAGTTAATAAGAGAGAATCACTTTAATGAGGAACTTTGGCTAATGCAGTTTATACCAAAACAACATTTCAGAAGATGCGCAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29725
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000031005 | Essential Splice Site | 441 | 542 | 15 | 18 |
| ENSDART00000147580 | Essential Splice Site | 526 | 627 | 15 | 18 |
Genomic Location (Zv9):
Chromosome 22 (position 10209694)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 10069862 |
| GRCz11 | 22 | 10099544 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAATCTGATGTTTGCGGCCCACAGTGGAGATGTTTCAGCTCTGAGGAGG[T/G]TACTTTATGCCACTCTCAACTTTTTCACTGTCAGTTTCTGACTGCTACCA
Long Flanking Sequence:
GCAGTTCTTCTGGTGGTGCCAAATGTGATGGGTGTCATGTGTTGGTCGCCCCCTGTGGACAAAGTCGGGAACAGTGTCCGTGGAATTCGCTTCTGTCAGGTGTTTCATTCATTGCTCTGCTAGTTTATTATCTAATTTTTAATTCCACACCATAGTTTTGATTATAAAAAAGTAATAACATAACTTTCCTTTTAAATAGGAACTGGTGTCTTTGTTCAACTTCCACAATTATGACAATCTGAGGCATTTTCTAAAGAAACAGGACCCTCGCAGGCAGTCTGGTGATGACAGAGTAAACTACAGCTTTCACATTAACACAGTTTGAAACTAAACTCCAATAATAAACACCAAAAGCCTGTGAAATGCCTAATTTTAAGCTATTTTTAGATAAGTTGTAAGCCTTGAGTAATAAACAAATTATATACTGCTTCTTGTAGAACAAGTCGGTGGTGAATCTGATGTTTGCGGCCCACAGTGGAGATGTTTCAGCTCTGAGGAGG[T/G]TACTTTATGCCACTCTCAACTTTTTCACTGTCAGTTTCTGACTGCTACCAAAATGTGCATTATTTACTTGTCTCCTGTTTTCTCCATCAGGTTTGCCCTGTCATCAATGAATATGGAGTTGAGGGACTATGACTCTCGTACACCTCTTCACGTAGCTGCTGCTGAAGGTAGACTTTTTCCTGTAAACGTGAAGCATATTTATGTGGTTTATTTATTCTTCAATCCAATTTGGCTTTCATGTCTGCTCTGTTTTAGGTCACGTGGATGTTGTGCTATTTTTAATACAGGCCTGCAAAGTCAACCCTTTTGTGAAAGACCGGTAAAGATTATTGGGTCACACTTTATTTTGCTGGTCTGTTTGTTGAATATAAGTTACATTGCATCTACATGCAAACTAATTCTCATTAGATTATGAGCAGACTGTTGGGCAAGGAGCAGTATCAGCAGATATTAAGCAGACAGTCTACTAATACTCAAATGGACCATTAAAATAAAGTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30726
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
A > G
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000031005 | Essential Splice Site | 488 | 542 | None | 18 |
| ENSDART00000147580 | Essential Splice Site | 573 | 627 | None | 18 |
Genomic Location (Zv9):
Chromosome 22 (position 10209123)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 22 | 10069291 |
| GRCz11 | 22 | 10098973 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTGCTTACCTTTAGCTAATCCATCAGATCTAAAACTAACCTCTGTCATTC[A/G]GGTGGGGAAATATTCCTCGAGACGATGCCATGCAGTTCGGGCAAAAGGAT
Long Flanking Sequence:
TCTCCTGTTTTCTCCATCAGGTTTGCCCTGTCATCAATGAATATGGAGTTGAGGGACTATGACTCTCGTACACCTCTTCACGTAGCTGCTGCTGAAGGTAGACTTTTTCCTGTAAACGTGAAGCATATTTATGTGGTTTATTTATTCTTCAATCCAATTTGGCTTTCATGTCTGCTCTGTTTTAGGTCACGTGGATGTTGTGCTATTTTTAATACAGGCCTGCAAAGTCAACCCTTTTGTGAAAGACCGGTAAAGATTATTGGGTCACACTTTATTTTGCTGGTCTGTTTGTTGAATATAAGTTACATTGCATCTACATGCAAACTAATTCTCATTAGATTATGAGCAGACTGTTGGGCAAGGAGCAGTATCAGCAGATATTAAGCAGACAGTCTACTAATACTCAAATGGACCATTAAAATAAAGTGTTACCGATTATTGTTTCTTTATTTGCTTACCTTTAGCTAATCCATCAGATCTAAAACTAACCTCTGTCATTC[A/G]GGTGGGGAAATATTCCTCGAGACGATGCCATGCAGTTCGGGCAAAAGGATGTTGTGAAGATCCTGGAGGAGTATGAGCAGACCTACAGCCCACAAACGTCTCAGACTGACACAGAAGATCTTAGTCAGCCATCCAAATGCTCATCTCTGGGGTGTAATCTGCTGTGAATCTATCAAACTAATGAACTAGTTGATTTCATGAAAATATGTGCAAAATTAGGGTACATTTATTAAAGTATCTCTCTAGAGTTCACTTTTTTCTATTTTGATTTGTAAATATTATAAAGATTTATATATATATATAATATAAGATTTATAATAAGTAAAAGATCTTTGTAAATTATTTGGGACATACCTGTTATCTTAGTGAAAAATGTACAGCAATGCACAATGTACAGTGTCTGACAAATAAAACCAAATATCCAAAAACGATTGGTATCTTCAAATATGTTTAAGCAGTGGGTATTTATGTTTTAATCTAATATCCAAGATTTTTTTTCA
Associated Phenotype:
Not determined